2,5-Dimetoksi-4-metilamfetamin

2,5-Dimetoksi-4-metilamfetamin
	1-(2,5-Dimetoksi-4-metilfenil)-2-aminopropan
Drugi nazivi	2,5-Dimetoksi-4-metilamfetamin
Identifikacija
CAS registarski broj	15588-95-1 [], (R): 43061-13-8; (S): 43061-14-9
PubChem	11735949
ChemSpider	9910656
ChEMBL	CHEMBL317634
Jmol-3D slike	{{#if:N[C@H](C)CC1=C(OC)C=C(C)C(OC)=C1 (R-isomer)O(c1cc(c(OC)cc1C[C@H](N)C)C)C\|Slika 1; Slika 2
SMILES
	N[C@H](C)CC1=C(OC)C=C(C)C(OC)=C1 (R-isomer) O(c1cc(c(OC)cc1C[C@H](N)C)C)C
InChI
	InChI=1S/C12H19NO2/c1-8-5-12(15-4)10(6-9(2)13)7-11(8)14-3/h5,7,9H,6,13H2,1-4H3/t9-/m1/s1 ; Kod: NTJQREUGJKIARY-SECBINFHSA-N InChI=1/C12H19NO2/c1-8-5-12(15-4)10(6-9(2)13)7-11(8)14-3/h5,7,9H,6,13H2,1-4H3/t9-/m1/s1; Kod: NTJQREUGJKIARY-SECBINFHBK
Svojstva
Molekulska formula	C12H19NO2
Molarna masa	209,29 g/mol
Tačka topljenja	61 °C, 334 K, 142 °F
	(šta je ovo?) (verifikuj) ; Ukoliko nije drugačije napomenuto, podaci se odnose na standardno stanje (25 °C, 100 kPa) materijala
	Infobox references

2,5-Dimetoksi-4-metilamfetamin (DOM; poznat kao STP od engl. Serenity, Tranquility, and Peace) je psihodelik i supstituisani amfetamin.^[5] DOM je klasifikovan kao kontrolisana supstanca u većini zemalja.^[6] On se generalno koristi oralnim putem.

Povezano

2,5-Dimetoksi-4-substituisani amfetamini

Reference

↑ Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit
↑ Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.
↑ Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit
↑ Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit
↑ Shulgin, Alexander; Ann Shulgin (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.
↑ „Green List: List of Psychotropic Substances Under International Control” (PDF). International Narcotics Control Board. August 2003 (23rd edition). str. 4. Arhivirano iz originala na datum 2012-08-31. Pristupljeno 28. 2. 2012.

Spoljašnje veze

Portal Hemija

[1] Li Q, Cheng T, Wang Y, Bryant SH (2010). „PubChem as a public resource for drug discovery.”. Drug Discov Today 15 (23-24): 1052-7. DOI:10.1016/j.drudis.2010.10.003. PMID 20970519. edit

[2] Evan E. Bolton, Yanli Wang, Paul A. Thiessen, Stephen H. Bryant (2008). „Chapter 12 PubChem: Integrated Platform of Small Molecules and Biological Activities”. Annual Reports in Computational Chemistry 4: 217-241. DOI:10.1016/S1574-1400(08)00012-1.

[3] Hettne KM, Williams AJ, van Mulligen EM, Kleinjans J, Tkachenko V, Kors JA. (2010). „Automatic vs. manual curation of a multi-source chemical dictionary: the impact on text mining”. J Cheminform 2 (1): 3. DOI:10.1186/1758-2946-2-3. PMID 20331846. edit

[4] Gaulton A, Bellis LJ, Bento AP, Chambers J, Davies M, Hersey A, Light Y, McGlinchey S, Michalovich D, Al-Lazikani B, Overington JP. (2012). „ChEMBL: a large-scale bioactivity database for drug discovery”. Nucleic Acids Res 40 (Database issue): D1100-7. DOI:10.1093/nar/gkr777. PMID 21948594. edit

[5] Shulgin, Alexander; Ann Shulgin (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.

[6] „Green List: List of Psychotropic Substances Under International Control” (PDF). International Narcotics Control Board. August 2003 (23rd edition). str. 4. Arhivirano iz originala na datum 2012-08-31. Pristupljeno 28. 2. 2012.

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